Total synthesis and herbicidal activity of natural rubrolides C, E and F-Reference-Cited by-同舟云学术

Total synthesis and herbicidal activity of natural rubrolides C, E and F

Published:2024-05-02 Issue: Volume: Page:1-10
ISSN:1478-6419
Container-title:Natural Product Research
language:en
Short-container-title:Natural Product Research

Author:

Gong Mengqiang¹,Cai Jinlong²,Lu Xingliang³,Zhou Xudong⁴,Li Junkai¹,Wu Qinglai¹,Wu Jianfeng⁵

Affiliation:

1. School of Agriculture, Yangtze University, Jingzhou, PRChina

2. Department of Environment and Life Science, Beijing University of Technology, Beijing, PRChina

3. School of Chemical and Biological Engineering, Lanzhou Jiaotong University, Lanzhou, PRChina

4. TCM and Ethnomedicine Innovation and Development Laboratory, School of Pharmacy, Hunan University of Chinese Medicine, Changsha, PRChina

5. State Key Laboratory of Toxicology and Medical Countermeasures and Laboratory of Toxicant Analysis, Institute of Pharmacology and Toxicology, Academy of Military Medical Sciences, Beijing, PRChina

Funder

National Natural Science Foundation of China

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/14786419.2024.2323544

Reference34 articles.

1. Phytogrowth- and photosynthesis-inhibiting properties of nostoclide analogues

2. Synthesis of Rubrolide Analogues as New Inhibitors of the Photosynthetic Electron Transport Chain

3. Evidence that cell survival is controlled by interleukin-3 independently of cell proliferation

4. Facile access to 4-aryl-2(5H)-furanones by Suzuki cross coupling: Efficient synthesis of rubrolides C and E

5. Targeted Isolation of Rubrolides from the New Zealand Marine Tunicate Synoicum kuranui

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